Job Summary

• Accountable for the scientific integrity of the study and the well-being of patients enrolled in one or more clinical trials, ensuring efficient and high-quality trial design.
• Responsible for timely delivery of a quality protocol, clinical execution of complex trials, and supports interpretation and communication of clinical trial data.
• Offers a competitive salary range, bonus target, long-term incentive program, and comprehensive benefits including 401(k), paid time off, and health coverage.

Matching Summary

Salary

Base: $176,600.00 - $294,300.00; Bonus/Equity: 20.0% bonus target and share-based long term incentive; Benefits: Comprehensive benefits package including 401(k), PTO, medical, dental, vision

Skills & Requirements

Key Requirements

• Advanced degree or professional certification
• 5+ years experience in biopharmaceutical industry
• Clinical research experience in phase 3/pivotal space
• Extensive knowledge of clinical development and regulations
• Demonstrated clinical, administrative, and project management capabilities
• Excellent verbal and written communication skills
• Demonstrated experience establishing, managing, and training teams

Work Rights